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Biosynthesis and Antimicrobial Activity of Semiconductor Nanoparticles against Oral Pathogens.

Bioinorganic chemistry and applications

Malarkodi C, Rajeshkumar S, Paulkumar K, Vanaja M, Gnanajobitha G, Annadurai G.
PMID: 24860280
Bioinorg Chem Appl. 2014;2014:347167. doi: 10.1155/2014/347167. Epub 2014 Mar 04.

Dental care is an essential phenomenon in human health. Oral pathogens can cause severe break which may show the way to serious issues in human disease like blood circulation and coronary disease. In the current study, we demonstrated the...

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Malarkodi C, Rajeshkumar S, Paulkumar K, et al. Biosynthesis and Antimicrobial Activity of Semiconductor Nanoparticles against Oral Pathogens. Bioinorg Chem Appl. 2014;2014:347167doi: 10.1155/2014/347167.
Malarkodi, C., Rajeshkumar, S., Paulkumar, K., Vanaja, M., Gnanajobitha, G., & Annadurai, G. (2014). Biosynthesis and Antimicrobial Activity of Semiconductor Nanoparticles against Oral Pathogens. Bioinorganic chemistry and applications, 2014347167. https://doi.org/10.1155/2014/347167
Malarkodi, C, et al. "Biosynthesis and Antimicrobial Activity of Semiconductor Nanoparticles against Oral Pathogens." Bioinorganic chemistry and applications vol. 2014 (2014): 347167. doi: https://doi.org/10.1155/2014/347167
Malarkodi C, Rajeshkumar S, Paulkumar K, Vanaja M, Gnanajobitha G, Annadurai G. Biosynthesis and Antimicrobial Activity of Semiconductor Nanoparticles against Oral Pathogens. Bioinorg Chem Appl. 2014;2014:347167. doi: 10.1155/2014/347167. Epub 2014 Mar 04. PMID: 24860280; PMCID: PMC4016845.
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SALMO and S3M: A Saliva Model and a Single Saliva Salt Model for Equilibrium Studies.

Bioinorganic chemistry and applications

Crea F, De Stefano C, Milea D, Pettignano A, Sammartano S.
PMID: 25733975
Bioinorg Chem Appl. 2015;2015:267985. doi: 10.1155/2015/267985. Epub 2015 Feb 04.

A model of synthetic saliva (SALMO, SALiva MOdel) is proposed for its use as standard medium in in vitro equilibrium and speciation studies of real saliva. The concentrations come out from the literature analysis of the composition of both...

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Crea F, De Stefano C, Milea D, et al. SALMO and S3M: A Saliva Model and a Single Saliva Salt Model for Equilibrium Studies. Bioinorg Chem Appl. 2015;2015:267985doi: 10.1155/2015/267985.
Crea, F., De Stefano, C., Milea, D., Pettignano, A., & Sammartano, S. (2015). SALMO and S3M: A Saliva Model and a Single Saliva Salt Model for Equilibrium Studies. Bioinorganic chemistry and applications, 2015267985. https://doi.org/10.1155/2015/267985
Crea, Francesco, et al. "SALMO and S3M: A Saliva Model and a Single Saliva Salt Model for Equilibrium Studies." Bioinorganic chemistry and applications vol. 2015 (2015): 267985. doi: https://doi.org/10.1155/2015/267985
Crea F, De Stefano C, Milea D, Pettignano A, Sammartano S. SALMO and S3M: A Saliva Model and a Single Saliva Salt Model for Equilibrium Studies. Bioinorg Chem Appl. 2015;2015:267985. doi: 10.1155/2015/267985. Epub 2015 Feb 04. PMID: 25733975; PMCID: PMC4334860.
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Antioxidant enzyme inhibitor role of phosphine metal complexes in lung and leukemia cell lines.

Bioinorganic chemistry and applications

Saygıdeğer Demir B, Keleş T, Serindağ O.
PMID: 25610346
Bioinorg Chem Appl. 2014;2014:717421. doi: 10.1155/2014/717421. Epub 2014 Dec 28.

Phosphine metal complexes have been recently evaluated in the field of cancer therapy. In this research, the cytotoxic effects of some metal phosphines {[PdCl2((CH2OH)2PCH2)2NCH3] (C1), [RuCl2(((CH2OH)2PCH2)2NCH3)2] (C2), [PtCl2((Ph2PCH2)2NCH3)(timin)2] (C3)} on K562 (human myelogenous leukemia cell line) and A549 (adenocarcinomic...

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Saygıdeğer Demir B, Keleş T, Serindağ O. Antioxidant enzyme inhibitor role of phosphine metal complexes in lung and leukemia cell lines. Bioinorg Chem Appl. 2014;2014:717421doi: 10.1155/2014/717421.
Saygıdeğer Demir, B., Keleş, T., & Serindağ, O. (2014). Antioxidant enzyme inhibitor role of phosphine metal complexes in lung and leukemia cell lines. Bioinorganic chemistry and applications, 2014717421. https://doi.org/10.1155/2014/717421
Saygıdeğer Demir, Burcu, et al. "Antioxidant enzyme inhibitor role of phosphine metal complexes in lung and leukemia cell lines." Bioinorganic chemistry and applications vol. 2014 (2014): 717421. doi: https://doi.org/10.1155/2014/717421
Saygıdeğer Demir B, Keleş T, Serindağ O. Antioxidant enzyme inhibitor role of phosphine metal complexes in lung and leukemia cell lines. Bioinorg Chem Appl. 2014;2014:717421. doi: 10.1155/2014/717421. Epub 2014 Dec 28. PMID: 25610346; PMCID: PMC4291011.
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Synthesis and Biological Evaluation of New Hydrazone Derivatives of Quinoline and Their Cu(II) and Zn(II) Complexes against Mycobacterium tuberculosis.

Bioinorganic chemistry and applications

Mandewale MC, Thorat B, Shelke D, Yamgar R.
PMID: 26759537
Bioinorg Chem Appl. 2015;2015:153015. doi: 10.1155/2015/153015. Epub 2015 Nov 25.

A new series of quinoline hydrazone derivatives and their metal complexes have been synthesized and their biological properties have been evaluated against Mycobacterium tuberculosis (H37 RV strain). Most of the newly synthesized compounds displayed 100% inhibitory activity at a...

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Mandewale MC, Thorat B, Shelke D, et al. Synthesis and Biological Evaluation of New Hydrazone Derivatives of Quinoline and Their Cu(II) and Zn(II) Complexes against Mycobacterium tuberculosis. Bioinorg Chem Appl. 2015;2015:153015doi: 10.1155/2015/153015.
Mandewale, M. C., Thorat, B., Shelke, D., & Yamgar, R. (2015). Synthesis and Biological Evaluation of New Hydrazone Derivatives of Quinoline and Their Cu(II) and Zn(II) Complexes against Mycobacterium tuberculosis. Bioinorganic chemistry and applications, 2015153015. https://doi.org/10.1155/2015/153015
Mandewale, Mustapha C, et al. "Synthesis and Biological Evaluation of New Hydrazone Derivatives of Quinoline and Their Cu(II) and Zn(II) Complexes against Mycobacterium tuberculosis." Bioinorganic chemistry and applications vol. 2015 (2015): 153015. doi: https://doi.org/10.1155/2015/153015
Mandewale MC, Thorat B, Shelke D, Yamgar R. Synthesis and Biological Evaluation of New Hydrazone Derivatives of Quinoline and Their Cu(II) and Zn(II) Complexes against Mycobacterium tuberculosis. Bioinorg Chem Appl. 2015;2015:153015. doi: 10.1155/2015/153015. Epub 2015 Nov 25. PMID: 26759537; PMCID: PMC4673354.
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Synthesis and Assessment of Antibacterial Activities of Ruthenium(III) Mixed Ligand Complexes Containing 1,10-Phenanthroline and Guanide.

Bioinorganic chemistry and applications

Abebe A, Hailemariam T.
PMID: 27833473
Bioinorg Chem Appl. 2016;2016:3607924. doi: 10.1155/2016/3607924. Epub 2016 Oct 19.

In this work, two complexes of ruthenium(III) ([Ru(phen)

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Abebe A, Hailemariam T. Synthesis and Assessment of Antibacterial Activities of Ruthenium(III) Mixed Ligand Complexes Containing 1,10-Phenanthroline and Guanide. Bioinorg Chem Appl. 2016;2016:3607924doi: 10.1155/2016/3607924.
Abebe, A., & Hailemariam, T. (2016). Synthesis and Assessment of Antibacterial Activities of Ruthenium(III) Mixed Ligand Complexes Containing 1,10-Phenanthroline and Guanide. Bioinorganic chemistry and applications, 20163607924. https://doi.org/10.1155/2016/3607924
Abebe, Atakilt, and Hailemariam, Tizazu. "Synthesis and Assessment of Antibacterial Activities of Ruthenium(III) Mixed Ligand Complexes Containing 1,10-Phenanthroline and Guanide." Bioinorganic chemistry and applications vol. 2016 (2016): 3607924. doi: https://doi.org/10.1155/2016/3607924
Abebe A, Hailemariam T. Synthesis and Assessment of Antibacterial Activities of Ruthenium(III) Mixed Ligand Complexes Containing 1,10-Phenanthroline and Guanide. Bioinorg Chem Appl. 2016;2016:3607924. doi: 10.1155/2016/3607924. Epub 2016 Oct 19. PMID: 27833473; PMCID: PMC5090073.
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A Comparison between Chemical Synthesis Magnetite Nanoparticles and Biosynthesis Magnetite.

Bioinorganic chemistry and applications

Kahani SA, Yagini Z.
PMID: 24982609
Bioinorg Chem Appl. 2014;2014:384984. doi: 10.1155/2014/384984. Epub 2014 Jun 01.

The preparation of Fe3O4 from ferrous salt by air in alkaline aqueous solution at various temperatures was proposed. The synthetic magnetites have different particle size distributions. We studied the properties of the magnetite prepared by chemical methods compared with...

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Kahani SA, Yagini Z. A Comparison between Chemical Synthesis Magnetite Nanoparticles and Biosynthesis Magnetite. Bioinorg Chem Appl. 2014;2014:384984doi: 10.1155/2014/384984.
Kahani, S. A., & Yagini, Z. (2014). A Comparison between Chemical Synthesis Magnetite Nanoparticles and Biosynthesis Magnetite. Bioinorganic chemistry and applications, 2014384984. https://doi.org/10.1155/2014/384984
Kahani, Seyed Abolghasem, and Yagini, Zahra. "A Comparison between Chemical Synthesis Magnetite Nanoparticles and Biosynthesis Magnetite." Bioinorganic chemistry and applications vol. 2014 (2014): 384984. doi: https://doi.org/10.1155/2014/384984
Kahani SA, Yagini Z. A Comparison between Chemical Synthesis Magnetite Nanoparticles and Biosynthesis Magnetite. Bioinorg Chem Appl. 2014;2014:384984. doi: 10.1155/2014/384984. Epub 2014 Jun 01. PMID: 24982609; PMCID: PMC4058688.
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Synthesis, Characterization, and Antifungal Studies of Cr(III) Complex of Norfloxacin and Bipiridyl Ligand.

Bioinorganic chemistry and applications

Debnath A, Hussain F, Masram DT.
PMID: 25276111
Bioinorg Chem Appl. 2014;2014:457478. doi: 10.1155/2014/457478. Epub 2014 Sep 03.

A novel slightly distorted octahedral complex of Cr(III) of norfloxacin (Nor) with the formula [Cr(III)(Nor)(Bipy)Cl2]Cl·2CH3OH has been synthesized hydrothermally in the presence of a N-containing heterocyclic compound 2,2'-bipyridyl (Bipy). The complex was characterized with FT-IR, elemental analysis, UV-visible spectroscopy,...

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Debnath A, Hussain F, Masram DT. Synthesis, Characterization, and Antifungal Studies of Cr(III) Complex of Norfloxacin and Bipiridyl Ligand. Bioinorg Chem Appl. 2014;2014:457478doi: 10.1155/2014/457478.
Debnath, A., Hussain, F., & Masram, D. T. (2014). Synthesis, Characterization, and Antifungal Studies of Cr(III) Complex of Norfloxacin and Bipiridyl Ligand. Bioinorganic chemistry and applications, 2014457478. https://doi.org/10.1155/2014/457478
Debnath, Anamika, et al. "Synthesis, Characterization, and Antifungal Studies of Cr(III) Complex of Norfloxacin and Bipiridyl Ligand." Bioinorganic chemistry and applications vol. 2014 (2014): 457478. doi: https://doi.org/10.1155/2014/457478
Debnath A, Hussain F, Masram DT. Synthesis, Characterization, and Antifungal Studies of Cr(III) Complex of Norfloxacin and Bipiridyl Ligand. Bioinorg Chem Appl. 2014;2014:457478. doi: 10.1155/2014/457478. Epub 2014 Sep 03. PMID: 25276111; PMCID: PMC4168151.
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The Improvement of the Resistance to Candida albicans and Trichophyton interdigitale of Some Woven Fabrics Based on Cotton.

Bioinorganic chemistry and applications

Surdu L, Stelescu MD, Manaila E, Nicula G, Iordache O, Dinca LC, Berechet MD, Vamesu M, Gurau D.
PMID: 25276112
Bioinorg Chem Appl. 2014;2014:763269. doi: 10.1155/2014/763269. Epub 2014 Sep 04.

This paper presents the improvement of the antimicrobial character of woven fabrics based on cotton. The woven fabrics were cleaned in oxygen plasma and treated by padding with silver chloride and titanium dioxide particles. The existence of silver and...

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Surdu L, Stelescu MD, Manaila E, et al. The Improvement of the Resistance to Candida albicans and Trichophyton interdigitale of Some Woven Fabrics Based on Cotton. Bioinorg Chem Appl. 2014;2014:763269doi: 10.1155/2014/763269.
Surdu, L., Stelescu, M. D., Manaila, E., Nicula, G., Iordache, O., Dinca, L. C., Berechet, M. D., Vamesu, M., & Gurau, D. (2014). The Improvement of the Resistance to Candida albicans and Trichophyton interdigitale of Some Woven Fabrics Based on Cotton. Bioinorganic chemistry and applications, 2014763269. https://doi.org/10.1155/2014/763269
Surdu, Lilioara, et al. "The Improvement of the Resistance to Candida albicans and Trichophyton interdigitale of Some Woven Fabrics Based on Cotton." Bioinorganic chemistry and applications vol. 2014 (2014): 763269. doi: https://doi.org/10.1155/2014/763269
Surdu L, Stelescu MD, Manaila E, Nicula G, Iordache O, Dinca LC, Berechet MD, Vamesu M, Gurau D. The Improvement of the Resistance to Candida albicans and Trichophyton interdigitale of Some Woven Fabrics Based on Cotton. Bioinorg Chem Appl. 2014;2014:763269. doi: 10.1155/2014/763269. Epub 2014 Sep 04. PMID: 25276112; PMCID: PMC4168144.
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Synthesis, Structural Characterization, and Biological Activity Studies of Ni(II) and Zn(II) Complexes.

Bioinorganic chemistry and applications

Kavitha P, Laxma Reddy K.
PMID: 24948904
Bioinorg Chem Appl. 2014;2014:568741. doi: 10.1155/2014/568741. Epub 2014 Apr 28.

Ni(II) and Zn(II) complexes were synthesized from tridentate 3-formyl chromone Schiff bases such as 3-((2-hydroxyphenylimino)methyl)-4H-chromen-4-one (HL1), 2-((4-oxo-4H-chromen-3-yl)methylneamino)benzoic acid (HL2), 3-((3-hydroxypyridin-2-ylimino)methyl)-4H-chromen-4-one (HL3), and 3-((2-mercaptophenylimino)methyl)-4H-chromen-4-one (HL4). All the complexes were characterized in the light of elemental analysis, molar conductance, FTIR, UV-VIS,...

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Kavitha P, Laxma Reddy K. Synthesis, Structural Characterization, and Biological Activity Studies of Ni(II) and Zn(II) Complexes. Bioinorg Chem Appl. 2014;2014:568741doi: 10.1155/2014/568741.
Kavitha, P., & Laxma Reddy, K. (2014). Synthesis, Structural Characterization, and Biological Activity Studies of Ni(II) and Zn(II) Complexes. Bioinorganic chemistry and applications, 2014568741. https://doi.org/10.1155/2014/568741
Kavitha, Palakuri, and Laxma Reddy, K. "Synthesis, Structural Characterization, and Biological Activity Studies of Ni(II) and Zn(II) Complexes." Bioinorganic chemistry and applications vol. 2014 (2014): 568741. doi: https://doi.org/10.1155/2014/568741
Kavitha P, Laxma Reddy K. Synthesis, Structural Characterization, and Biological Activity Studies of Ni(II) and Zn(II) Complexes. Bioinorg Chem Appl. 2014;2014:568741. doi: 10.1155/2014/568741. Epub 2014 Apr 28. PMID: 24948904; PMCID: PMC4022167.
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Biosorption of Arsenic(III) from Aqueous Solutions by Modified Fungal Biomass of Paecilomyces sp.

Bioinorganic chemistry and applications

Acosta Rodríguez I, Martínez-Juárez VM, Cárdenas-González JF, Moctezuma-Zárate Mde G.
PMID: 24235911
Bioinorg Chem Appl. 2013;2013:376780. doi: 10.1155/2013/376780. Epub 2013 Oct 23.

The biosorption of As(III) on iron-coated fungal biomass of Paecilomyces sp. was studied in this work. It was found that the biomass was very efficient removing the metal in solution, using Atomic Absorption, reaching the next percentage of removals:...

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Acosta Rodríguez I, Martínez-Juárez VM, Cárdenas-González JF, et al. Biosorption of Arsenic(III) from Aqueous Solutions by Modified Fungal Biomass of Paecilomyces sp. Bioinorg Chem Appl. 2013;2013:376780doi: 10.1155/2013/376780.
Acosta Rodríguez, I., Martínez-Juárez, V. M., Cárdenas-González, J. F., & Moctezuma-Zárate, M. d. e. . G. (2013). Biosorption of Arsenic(III) from Aqueous Solutions by Modified Fungal Biomass of Paecilomyces sp. Bioinorganic chemistry and applications, 2013376780. https://doi.org/10.1155/2013/376780
Acosta Rodríguez, Ismael, et al. "Biosorption of Arsenic(III) from Aqueous Solutions by Modified Fungal Biomass of Paecilomyces sp." Bioinorganic chemistry and applications vol. 2013 (2013): 376780. doi: https://doi.org/10.1155/2013/376780
Acosta Rodríguez I, Martínez-Juárez VM, Cárdenas-González JF, Moctezuma-Zárate Mde G. Biosorption of Arsenic(III) from Aqueous Solutions by Modified Fungal Biomass of Paecilomyces sp. Bioinorg Chem Appl. 2013;2013:376780. doi: 10.1155/2013/376780. Epub 2013 Oct 23. PMID: 24235911; PMCID: PMC3819882.
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Syntheses, Characterization, Thermal, and Antimicrobial Studies of Lanthanum(III) Tolyl/Benzyldithiocarbonates.

Bioinorganic chemistry and applications

Andotra S, Kalgotra N, Pandey SK.
PMID: 24817836
Bioinorg Chem Appl. 2014;2014:780631. doi: 10.1155/2014/780631. Epub 2014 Apr 09.

Lanthanum(III) tris(O-tolyl/benzyldithiocarbonates), [La(ROCS2)] (R = o-, m-, p-CH3C6H4 and C6H5CH2), were isolated as yellow solid by the reaction of LaCl3 ·7H2O with sodium salt of tolyl/benzyldithiocarbonates, ROCS2Na (R = o-, m-, p-CH3C6H4 and C6H5CH2), in methanol under anhydrous conditions...

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Andotra S, Kalgotra N, Pandey SK. Syntheses, Characterization, Thermal, and Antimicrobial Studies of Lanthanum(III) Tolyl/Benzyldithiocarbonates. Bioinorg Chem Appl. 2014;2014:780631doi: 10.1155/2014/780631.
Andotra, S., Kalgotra, N., & Pandey, S. K. (2014). Syntheses, Characterization, Thermal, and Antimicrobial Studies of Lanthanum(III) Tolyl/Benzyldithiocarbonates. Bioinorganic chemistry and applications, 2014780631. https://doi.org/10.1155/2014/780631
Andotra, Savit, et al. "Syntheses, Characterization, Thermal, and Antimicrobial Studies of Lanthanum(III) Tolyl/Benzyldithiocarbonates." Bioinorganic chemistry and applications vol. 2014 (2014): 780631. doi: https://doi.org/10.1155/2014/780631
Andotra S, Kalgotra N, Pandey SK. Syntheses, Characterization, Thermal, and Antimicrobial Studies of Lanthanum(III) Tolyl/Benzyldithiocarbonates. Bioinorg Chem Appl. 2014;2014:780631. doi: 10.1155/2014/780631. Epub 2014 Apr 09. PMID: 24817836; PMCID: PMC4000956.
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Stabilization of submicron calcium oxalate suspension by chondroitin sulfate C may be an efficient protection from stone formation.

Bioinorganic chemistry and applications

Li JJ, Xue JF, Ouyang JM.
PMID: 24382950
Bioinorg Chem Appl. 2013;2013:360142. doi: 10.1155/2013/360142. Epub 2013 Dec 08.

The influences of chondroitin sulfate C (C6S) on size, aggregation, sedimentation, and Zeta potential of sub-micron calcium oxalate monohydrate (COM) and calcium oxalate dihydrate (COD) crystallites with mean sizes of about 330 nm were investigated using an X-ray diffractometer,...

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Li JJ, Xue JF, Ouyang JM. Stabilization of submicron calcium oxalate suspension by chondroitin sulfate C may be an efficient protection from stone formation. Bioinorg Chem Appl. 2013;2013:360142doi: 10.1155/2013/360142.
Li, J. J., Xue, J. F., & Ouyang, J. M. (2013). Stabilization of submicron calcium oxalate suspension by chondroitin sulfate C may be an efficient protection from stone formation. Bioinorganic chemistry and applications, 2013360142. https://doi.org/10.1155/2013/360142
Li, Jun-Jun, et al. "Stabilization of submicron calcium oxalate suspension by chondroitin sulfate C may be an efficient protection from stone formation." Bioinorganic chemistry and applications vol. 2013 (2013): 360142. doi: https://doi.org/10.1155/2013/360142
Li JJ, Xue JF, Ouyang JM. Stabilization of submicron calcium oxalate suspension by chondroitin sulfate C may be an efficient protection from stone formation. Bioinorg Chem Appl. 2013;2013:360142. doi: 10.1155/2013/360142. Epub 2013 Dec 08. PMID: 24382950; PMCID: PMC3870629.
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Showing 1 to 12 of 564 entries